ライフサイエンスコーパス: thermophilic

1 89% in the mesophilic reactor and 85% in the thermophilic.

2 We operated six thermophilic (55 degrees C) bioreactors to test how the

3 Here, we show that the Ech complex of the thermophilic acetogenic bacterium Thermoanaerobacter kiv

4 The recently discovered thermophilic acidobacterium Candidatus Chloracidobacteri

5 The genome of the thermophilic actinobacterium Thermobifida fusca encodes

6 ysis of the recently sequenced genome of the thermophilic actinomycete Thermobifida fusca revealed an

7 ynamics are investigated in two mutants of a thermophilic alcohol dehydrogenase (ht-ADH): Y25A (at th

8 A tetrameric thermophilic alcohol dehydrogenase from Bacillus stearot

9 function of temperature in two variants of a thermophilic alcohol dehydrogenase: W87F and W87F:H43A.

10 ransfer step catalyzed by a series of mutant thermophilic alcohol dehydrogenases (ht-ADH), presenting

11 The thermophilic alga C. merolae thrives in extreme environm

12 Naegleria fowleri is a climate-sensitive, thermophilic ameba found in the environment, including w

13 Naegleria fowleri is a climate-sensitive, thermophilic ameba found in warm, freshwater lakes and r

14 iter, is the highest reported thus far for a thermophilic anaerobe, although further improvements are

15 gain insights into mannan degradation by the thermophilic anaerobic bacterium Caldanaerobius polysacc

16 oxidation activator protein (CooA) from the thermophilic anaerobic bacterium Carboxydothermus hydrog

17 ing Thermoanaerobacterium saccharolyticum, a thermophilic anaerobic bacterium that ferments xylan and

18 Clostridium thermocellum is a thermophilic anaerobic bacterium that rapidly solubilize

19 ith 100 mM of [2-(13)C] sodium acetate under thermophilic anaerobic conditions.

20 s and intI1 decreased in all microcosms, but thermophilic anaerobic digestion, alkaline stabilization

21 c digestion, mesophilic anaerobic digestion, thermophilic anaerobic digestion, pasteurization, and al

22 g insight into the physiology and ecology of thermophilic anaerobic methanotrophy and suggesting that

23 ial capability, and acetotrophic pathways in thermophilic anaerobic reactors.

24 The host, Marinitoga piezophila is a thermophilic, anaerobic and piezophilic bacterium isolat

25 ) (ATCC BAA-2073, JCM 16842) is an extremely thermophilic, anaerobic bacterium capable of hydrolyzing

26 Clostridium thermocellum DSM1313 is a thermophilic, anaerobic bacterium with some of the highe

27 We began with the thermophilic, anaerobic, cellulolytic bacterium Caldicel

28 Marinitoga piezophila KA3 is a thermophilic, anaerobic, chemoorganotrophic, sulfur-redu

29 e candidate SAM-I riboswitches isolated from thermophilic and cryophilic bacteria.

30 lap between quinone compositions of distinct thermophilic and halophilic archaea and bacteria may ind

31 Proteins from thermophilic and hyperthermophilic organisms are stable

32 Furthermore, the samples from thermophilic and mesophilic codigesters had different DO

33 res distinguish intersubunit linkages of the thermophilic and mesophilic enzyme Bacillus subtilis cho

34 P and plays an adaptive role in catalysis by thermophilic and mesophilic enzymes.

35 gn chimeric proteins by hybridizing EIC from thermophilic and mesophilic organisms, and we characteri

36 thermal growth rate data obtained in a dozen thermophilic and mesophilic organisms.

37 the evolutionarily distant F-type motors of thermophilic and mesophilic origins, and they differ onl

38 mophilic enzyme, suggesting that hybridizing thermophilic and mesophilic proteins is a valid strategy

39 ndant in crenarchaeota, which thrive in both thermophilic and nonthermophilic environments, with wide

40 upport the notions that Precambrian life was thermophilic and that proteins can evolve from substrate

41 Here we examine mesophilic to thermophilic AOM in hydrothermal sediments recovered fro

42 ethods the number of viruses identified from thermophilic Archaea and Bacteria is still very small.

43 oses the process of allopatric speciation in thermophilic Archaea and brings us closer to a generaliz

44 , our ability to explore the cell biology of thermophilic archaea has been limited by the technical c

45 Two thermophilic archaea, strain PK and strain MG, were isol

46 In thermophilic archaea, the HerA helicase and NurA nucleas

47 In thermophilic archaea, the Mre11 and Rad50 genes cluster

48 or the repair of double-strand DNA breaks in thermophilic archaea.

49 ole in thermostabilization compared with the thermophilic archaea.

50 eotide binding to the HerA-NurA complex from thermophilic archaea.

51 evidence that four different mesophilic and thermophilic archaeal RNase P holoenzymes, reconstituted

52 Here we report a role for the thermophilic archaeal Sulfolobus solfataricus SSB (SsoSS

53 ane calcium-activated potassium channel from thermophilic archaebacteria.

54 re, we report the structure of Dim1 from the thermophilic archaeon Methanocaldococcus jannaschii.

55 ted in vitro the RNase P holoenzyme from the thermophilic archaeon Pyrococcus furiosus (Pfu) and furt

56 studies on the DNA alkyltransferase from the thermophilic archaeon Sulfolobus solfataricus (SsOGT).

57 2, and the topoisomerase 3, SsTop3, from the thermophilic archaeon Sulfolobus solfataricus.

58 a novel, low molecular weight TrxR from the thermophilic archaeon Thermoplasma acidophilum ( taTrxR)

59 e characterization of an RNA ligase from the thermophilic archaeon, Methanobacterium thermoautotrophi

60 t exploits protein engineering to "humanise" thermophilic archeal surrogate proteins as targets for s

61 conditions that allow direct comparison to a thermophilic (B. stearothermophilus) ortholog, Ec-DHFR a

62 Thermophilic Bacillus altitudinis immobilized nanodiamon

63 The catalytic chemistry of the thermophilic Bacillus stearothermophilus alcohol dehydro

64 uridine at position 54 stabilizes tRNAs from thermophilic bacteria and hyperthermophilic archaea and

65 the physiology and biochemistry of anaerobic thermophilic bacteria and, more lately, to anaerobic fun

66 ral other described hemicellulose-fermenting thermophilic bacteria can only partially utilize this GA

67 r instance with a cluster of sulfur-reducing thermophilic bacteria coming together irrespective of th

68 pendent from the availability of substrates, thermophilic bacteria dominated microcosms that were inc

69 Phenol hydroxylase gene cloning from the thermophilic bacteria Geobacillus thermoglucosidasius wa

70 Extremely thermophilic bacteria of the genus Caldicellulosiruptor

71 esent the crystal structure of BamD from the thermophilic bacteria Rhodothermus marinus refined to 2.

72 We reasoned that thermophilic bacteria would be a good source for well-be

73 antigens ranging from avian excreta, fungi, thermophilic bacteria, and protozoa to reactive chemical

74 the isolated HisF TIM barrel domain from the thermophilic bacteria, Thermotoga maritima, enabled an N

75 med on Escherichia coli RecA and RecA from a thermophilic bacteria, Thermus thermophilus.

76 ive features as F1 from Escherichia coli and thermophilic bacteria.

77 c bacterial genera analyzed, but absent from thermophilic bacteria.

78 nced yield and tailor-made EPS production by thermophilic bacteria.

79 history between RNases H from mesophilic and thermophilic bacteria.

80 cycle of F1-ATPase, mostly based on F1 from thermophilic bacteria.

81 A search of five thermophilic bacterial genomes identified a coded amino

82 by species in the noncellulosomal, extremely thermophilic bacterial genus Caldicellulosiruptor.

83 res of the large terminase nuclease from the thermophilic bacteriophage G20c show that it is most sim

84 Here we identified gp83 of the thermophilic bacteriophage P74-26 as the TerS protein.

85 Here, we show that photosystem I from a thermophilic bacterium and cytochrome-c(6) can, in combi

86 Thermobifida fusca is a moderately thermophilic bacterium and holds high biocatalytic poten

87 ve determined the structure of NusB from the thermophilic bacterium Aquifex aeolicus and studied the

88 temperatures, we sequenced the genome of the thermophilic bacterium Caldanaerobius polysaccharolyticu

89 The thermophilic bacterium Caldicellulosiruptor bescii uses

90 The genome of the extremely thermophilic bacterium Caldicellulosiruptor kronotskyens

91 ystal structures of a Group III CPN from the thermophilic bacterium Carboxydothermus hydrogenoformans

92 dihydrofolate reductase from the moderately thermophilic bacterium Geobacillus stearothermophilus (B

93 cterized a thermostable NOS homolog from the thermophilic bacterium Geobacillus stearothermophilus (g

94 Here, we show that the Cas9 protein from the thermophilic bacterium Geobacillus stearothermophilus (G

95 Strains of the Gram-positive, thermophilic bacterium Geobacillus stearothermophilus po

96 a nisin analog encoded on the genome of the thermophilic bacterium Geobacillus thermodenitrificans N

97 hosphogluconate dehydrogenase (6PGDH) from a thermophilic bacterium Moorella thermoacetica with rever

98 xide/oxygen binding (H-NOX) protein from the thermophilic bacterium Thermoanaerobacter tengcongensis,

99 teractions of SmpB.SsrA orthologues from the thermophilic bacterium Thermoanaerobacter tengcongensis.

100 glC ORF encoding a beta-glucosidase from the thermophilic bacterium Thermobifida fusca and inserted i

101 An ArsI ortholog, TcArsI, from the thermophilic bacterium Thermomonospora curvata was expre

102 an extensive and diverse sugar kinome in the thermophilic bacterium Thermotoga maritima.

103 n of gene expression during infection of the thermophilic bacterium Thermus thermophilus HB8 with the

104 T4P and natural transformation of DNA in the thermophilic bacterium Thermus thermophilus requires a u

105 interacting mutations in the ribosome of the thermophilic bacterium Thermus thermophilus.

106 sis of replication fidelity in the extremely thermophilic bacterium Thermus thermophilus.

107 he dioxygen complex of the NOS enzyme from a thermophilic bacterium, Geobacillus stearothermophilus (

108 a Gram-positive, spore-forming, aerobic and thermophilic bacterium, isolated from a soil sample obta

109 nteract with one another to generate extreme thermophilic behavior and are responsible for approximat

110 hat three residues in the active site of the thermophilic beta-1,4-xylanase from Nonomuraea flexuosa

111 d to ferment milk to obtain yogurt belong to thermophilic, bile-sensitive species of lactic acid bact

112 enes creates unprecedented opportunities for thermophilic bioalcohol production.

113 Thermophilic Bst DNA polymerase had the highest specific

114 gment, 3'-->5' exo(-) Klenow DNA polymerase, thermophilic Bst DNA polymerase large fragment, Thermina

115 Thermostable enzymes and thermophilic cell factories may afford economic advantag

116 s by the Firmicutes and Bacteroidetes in the thermophilic cellulolytic consortia is proposed.

117 ocellum wild-type strain YS is an anaerobic, thermophilic, cellulolytic bacterium capable of directly

118 Caldicellulosiruptor bescii is an extremely thermophilic, cellulolytic bacterium with a growth optim

119 Clostridium thermocellum is an anaerobic, thermophilic, cellulolytic, and ethanogenic bacterium.

120 owth optimum at 78 degrees C and is the most thermophilic cellulose degrader known.

121 These values reflect the thermophilic characteristics of the UVrABC nuclease comp

122 icus UBT1 has been described as a moderately thermophilic chemolithoautotroph with a novel nitrogenas

123 II RubisCO functions in the CBB cycle in the thermophilic chemolithoautotrophic bacterium Thermodesul

124 ntigs from an in situ-enriched cellulolytic, thermophilic community.

125 rich source for additional investigations of thermophilic composting microbiology.

126 Under thermophilic conditions (60 degrees C), T. pseudethanoli

127 to microcrystalline cellulose under aerobic, thermophilic conditions using green waste compost as the

128 At thermophilic conditions, a higher efficiency of CH4 prod

129 artial pressure between 0.25 and 1 atm under thermophilic conditions.

130 re specifically adapted to switchgrass under thermophilic conditions.

131 phisticated systems for its adaptation under thermophilic conditions.

132 figuration was tested at both mesophilic and thermophilic conditions.

133 e Mediterranean which studied the widespread thermophilic conifer Pinus halepensis and involved 157 p

134 The Y-family DNA polymerase Dpo4, from the thermophilic crenarchaeon Sulfolobus solfataricus P2, of

135 overy of ammonia oxidation by mesophilic and thermophilic Crenarchaeota and the widespread distributi

136 A study on thermophilic cyanobacteria reveals how environmentally i

137 enomes of the two closely related freshwater thermophilic cyanobacteria Synechococcus sp. strain JA-3

138 re we describe a novel pair of Phys from two thermophilic cyanobacteria, Synechococcus sp. OS-A and O

139 ly available crystal structures of PSII from thermophilic cyanobacteria.

140 Using thermophilic cyanobacterial homologs, we solve crystal s

141 The genomes of two closely related thermophilic cyanobacterial isolates, designated Synecho

142 Deep sequencing of a thermophilic cyanobacterial population and analysis of t

143 e discovered a tetrameric form of PSI in the thermophilic cyanobacterium Chroococcidiopsis sp TS-821

144 bsorption by JSC1_58120g3, a frCBCR from the thermophilic cyanobacterium Leptolyngbya sp. JSC-1 that

145 highly active dimeric b(6)f complex from the thermophilic cyanobacterium Thermosynechococcus elongatu

146 agnesium chelatase H subunit, ChlH, from the thermophilic cyanobacterium Thermosynechococcus elongatu

147 ize the cyanobacteriochrome Tlr0924 from the thermophilic cyanobacterium Thermosynechococcus elongatu

148 ructure of the 0.42-MDa NDH complex from the thermophilic cyanobacterium Thermosynechococcus elongatu

149 cally improve the orientation of PSII from a thermophilic cyanobacterium, Thermosynechococcus elongat

150 Unfolding thermodynamics of a thermophilic cytochrome c552 from Hydrogenobacter thermo

151 tions in the substrate binding region of the thermophilic cytochrome P450 enzyme CYP119.

152 nd finally, how he extended these studies to thermophilic desert ants in other deserts of the world,

153 centered on Cataglyphis have rendered these thermophilic desert ants model organisms in the study of

154 are either unchanged or more flexible in the thermophilic DHFR from B. stearothermophilus.

155 y (HDX-MS) as a function of temperature in a thermophilic dihydrofolate reductase from Bacillus stear

156 rmincola ferriacetica is a recently isolated thermophilic, dissimilatory Fe(III)-reducing, Gram-posit

157 rporated into DNA by selected mesophilic and thermophilic DNA polymerases and the resulting primer ex

158 In planta expression of a thermophilic endoglucanase (AcCel5A) reduces recalcitran

159 Thermophilic endospores are widespread in cold marine se

160 To test whether thermophilic endospores can survive prolonged exposure t

161 milar communities were observed in companion thermophilic enrichments on insoluble wheat arabinoxylan

162 cus primase may represent an adaptation to a thermophilic environment.

163 nzyme from E. coli (EcDHFR) and the dimeric, thermophilic enzyme from Thermotoga maritima (TmDHFR).

164 rmostable and more active than the wild-type thermophilic enzyme, suggesting that hybridizing thermop

165 ponding mesophilic (Ms) enzymes, because the thermophilic enzymes are less flexible (assuming that fl

166 ion in mesophiles can be aided by the use of thermophilic enzymes as starting points for protein desi

167 ngle-molecule measurements of mesophilic and thermophilic enzymes at 70 degrees C.

168 t low temperature, they are faster than some thermophilic enzymes at high temperature.

169 ons presume that the reduced dynamics of the thermophilic enzymes is the reason for their reduced cat

170 g kinetic stabilization as observed for some thermophilic enzymes.

171 idues, in contrast with previously described thermophilic enzymes.

172 ndicates that strain WSUCF1 has promise as a thermophilic EPS producer for a broad range of industria

173 studies of RNA polymerases (RNAPs) from the thermophilic eubacteria Thermus aquaticus (Taq) and Ther

174 ttle is known about nucleoid organization in thermophilic eubacteria.

175 -GlcNAc cycling enzymes in the genome of the thermophilic eubacterium Thermobaculum terrenum.

176 ved crystal structures of free CRM1 from the thermophilic eukaryote Chaetomium thermophilum.

177 e, these genomes are the first described for thermophilic eukaryotes and the first complete telomere-

178 obacter pseudethanolicus 39E (ATCC 33223), a thermophilic, Fe(III)-reducing, and fermentative bacteri

179 cyanobacterium Synechocystis PCC6803 and the thermophilic, fermentative bacterium Pelotomaculum therm

180 ponse to the nonconserved E77 present in the thermophilic Fpg sequences used for the crystallography

181 ntral nervous system infection caused by the thermophilic free-living ameba Naegleria fowleri.

182 potential reservoir of thermostable enzymes, thermophilic fungi are amenable to manipulation using cl

183 e we describe and compare the genomes of two thermophilic fungi, Myceliophthora thermophila and Thiel

184 the junction-resolving enzyme GEN1 from the thermophilic fungus Chaetomium thermophilum and expresse

185 res of the separase protease domain from the thermophilic fungus Chaetomium thermophilum, alone or co

186 e most stable parent, CBH II enzyme from the thermophilic fungus Humicola insolens, which suggests th

187 estigated two related Dicer enzymes from the thermophilic fungus Sporotrichum thermophile.

188 Thermophilic fungus Thermoascus aurantiacus (CBMAI 756)

189 We characterized a novel BVMO from the thermophilic fungus Thermothelomyces thermophila, determ

190 n, which binds the motor heavy chain, from a thermophilic fungus.

191 rt the previously unexplored capabilities of thermophilic Geobacillus sp. strain WSUCF1 to generate e

192 is the first report on genome analysis of a thermophilic Geobacillus species focusing on its EPS bio

193 rAB is a heterodimeric ABC exporter from the thermophilic Gram-negative eubacterium Thermus thermophi

194 complex, and the reaction center (RC) in the thermophilic green phototrophic bacterium Chloroflexus a

195 ne boundary, while trans-Arctic dispersal in thermophilic groups may have been limited to the early E

196 e because it is halophilic, alkaliphilic and thermophilic, growing optimally at 3.5 M Na(+), pH(55 de

197 s in the lake, including both mesophilic and thermophilic habitats, had multiple virophage genotypes.

198 ion/proton antiporters in the genome of this thermophilic haloalkaliphile.

199 the consensus sequences of single repeats of thermophilic HEAT (PBS_HEAT) and Leucine-Rich Variant (L

200 mined the crystal structure of DGGR from the thermophilic heterotrophic archaea Thermoplasma acidophi

201 and high temperature unfolding kinetics of a thermophilic homolog, Thermobifida fusca protease A (TFP

202 t thermal constraints by adding a moderately thermophilic homologue to the previously characterized m

203 o has a surprisingly low DeltaC(p), like the thermophilic homologue.

204 end the frontier of metabolic engineering in thermophilic hosts, have the potential to significantly

205 c complementation of yeast with prokaryotic, thermophilic IGPS.

206 -hairpin that is unique in the structures of thermophilic inteins.

207 experimental biogas plant composed of three thermophilic leach bed reactors (51-56 degrees C) follow

208 etate formation at different OLRs within the thermophilic leach bed reactors as well as a negligible

209 umber of organisms with photoautotrophic and thermophilic lifestyles.

210 while the folding core region determines the thermophilic-like behavior of this family of proteins, t

211 th the termination of conditions required by thermophilic lineages.

212 Archaea such as Metallosphaera sedula are thermophilic lithoautotrophs that occupy unusually acidi

213 y enhancing the mechanistic understanding of thermophilic lithoautotrophy.

214 ly been solved to 3.0-A resolution using the thermophilic Mastigocladus laminosus whose genome has no

215 Agr-type cyclic peptide to be produced by a thermophilic member of the Firmicutes.

216 genome of strain Exiguobacterium sp. AT1b, a thermophilic member of the genus Exiguobacterium whose r

217 Interestingly, we also present a hybrid thermophilic/mesophilic enzyme that is thermostable and

218 studies that have suggested that, in certain thermophilic microbes, disulfide bonds play a key role i

219 tabilizing intracellular proteins in certain thermophilic microbes.

220 izing beta-1,4-galactosidase activity from a thermophilic microbial community lysate.

221 45 degrees C) resulted in the emergence of a thermophilic microbial community specialized in fermenta

222 rganism, Herbinix spp. strain LL1355, from a thermophilic microbiome that can consume 85% of the reca

223 The alpha-galactosidase AgaA from the thermophilic microorganism Geobacillus stearothermophilu

224 The use of thermophilic microorganisms as biocatalysts for electrom

225 iments of the Guaymas Basin are inhabited by thermophilic microorganisms, including anaerobic methane

226 cations of phenotype arrays to anaerobic and thermophilic microorganisms, use of the plates in stress

227 phobic proteins in soluble stable forms with thermophilic minichaperone, GroEL apical domain (GrAD) a

228 (Moapa coriacea) is a critically endangered thermophilic minnow native to the Muddy River ecosystem

229 Thermus thermophilus is a thermophilic model organism distantly related to the mes

230 anosarcina mazei Go1 A-ATP synthase, and the thermophilic motor alpha3beta3gamma, from Geobacillus st

231 site loops at the mesophilic ScOMPDC and the thermophilic MtOMPDC.

232 Clostridium thermocellum is a thermophilic, obligately anaerobic, gram-positive bacter

233 ect numerous redox enzymes, particularly for thermophilic ones, which can generate NAD(P)H reacted wi

234 two mutations per genome per replication for thermophilic ones.

235 In particular, it has been suggested that thermophilic or hyperthermophilic (Tm) enzymes have lowe

236 to design RNases H that display the desired thermophilic or mesophilic properties, as defined by the

237 hydrogenotrophic methanogenesis pathway in a thermophilic order of the Verstraetearchaeota, which we

238 Here we report that P450s derived from a thermophilic organism and containing an iridium porphyri

239 [a]P-N2-dG (G*), by UvrABC nuclease from the thermophilic organism Bacillus caldotenax was investigat

240 from the mesophilic organism E. coli and the thermophilic organism T. thermophilus.

241 :quinone oxidoreductase (complex I) from the thermophilic organism Thermus thermophilus HB8 has been

242 Cel7A from the thermophilic organism was moderately more activated by t

243 t species to predict which comes from a more thermophilic organism, with accuracy ranging from 0.538

244 rium did not fix nitrogen and probably was a thermophilic organism.

245 plain the high optimal growth temperature in thermophilic organisms and are in excellent quantitative

246 Proteins from thermophilic organisms are able to function under condit

247 ochondrial carriers from both mesophilic and thermophilic organisms exhibit poor stability in mild de

248 coming limitations include sourcing CAs from thermophilic organisms, using protein engineering to evo

249 proteins from psychrophilic, mesophilic, or thermophilic organisms.

250 grees C, which is more akin to proteins from thermophilic organisms.

251 the previously characterized mesophilic and thermophilic pair.

252 Interglacial deposits contain thermophilic palms suggesting warm and wet climates.

253 For the most part, thermophilic patterns in the genome and proteome of A. c

254 -26), revealing key differences between this thermophilic phage and its mesophilic counterparts.

255 DNA binding and cleavage using TerL from the thermophilic phage P74-26.

256 bacterial RNAP-binding proteins encoded by a thermophilic phage.

257 g point, Bryant et al. have discovered a new thermophilic phototroph from a poorly characterized bact

258 genus Caldicellulosiruptor contains the most thermophilic, plant biomass-degrading bacteria isolated

259 This composting exhibits a sustained thermophilic profile (50 degrees C to 75 degrees C), whi

260 However, previously studied pAgos from thermophilic prokaryotes function at elevated temperatur

261 ), we discovered three related proteins from thermophilic prokaryotes, which we grouped into a novel

262 hioarsenate species transformation by (hyper)thermophilic prokaryotes.

263 The moderately thermophilic protein has a melting temperature (T(m)) si

264 on of the MD trajectories indicates that the thermophilic protein samples conformations productive fo

265 low the same unfolding pathway, but with the thermophilic protein showing much slower unfolding.

266 capacity upon unfolding (DeltaC(p)) for the thermophilic protein.

267 derstand the origin of enhanced stability in thermophilic proteins by analyzing thermodynamic data fo

268 ise comparisons of homologous mesophilic and thermophilic proteins can help to identify the energetic

269 structural features normally associated with thermophilic proteins such as an increase in salt bridge

270 re to understand the dynamical properties of thermophilic proteins under pressure.

271 d state is encoded in the sequences of these thermophilic proteins, we subjected the RNase H from Chl

272 idual structure in the unfolded state of the thermophilic proteins.

273 cellulase enzyme, an endoglucanase from the thermophilic Pyrococcus horikoshii.

274 Cel7A) from mesophilic Hypocrea jecorina and thermophilic Rasamsonia emersonii and two variants of th

275 ow fiber membrane (HFM) module in continuous thermophilic reactors, CO did not inhibit the process ev

276 was almost no phycobilisome mobility in the thermophilic red alga Cyanidium caldarium that was not c

277 unction in mesophilic red algae; however, in thermophilic red algae, this process is replaced by nonp

278 antennae can be regulated in mesophilic and thermophilic red algae.

279 stablishes a system to comprehensively study thermophilic replisomes and evolutionary links between a

280 emical attractants E. coli exhibits a steady thermophilic response, the magnitude of which decreases

281 ormational basis for reduced activity of the thermophilic ribonuclease HI enzyme from Thermus thermop

282 In this work, we describe the ability of the thermophilic RNA ligase MthRnl from Methanobacterium the

283 In reported structures of thermophilic RNA polymerase, the G1249 residue is locate

284 Thermobifida fusca is a moderately thermophilic soil bacterium that belongs to Actinobacter

285 he genome of Heliobacterium modesticaldum, a thermophilic species belonging to this unique group of p

286 sed as abrupt shifts to regimes dominated by thermophilic species.

287 se trends in SRR, members of the potentially thermophilic, spore-forming, Desulfotomaculum were detec

288 Thermophilic sulfate reduction, however, had a higher ac

289 Dpo4, an archetypal Y-family member from the thermophilic Sulfolobus solfataricus, was used to extend

290 Sac10b homologs in thermophilic Sulfolobus species are very abundant.

291 Our work highlights a thermophilic system for studying the role of small termi

292 ferences in the catalytic parameters between thermophilic Thermus aquaticus and mesophilic Deinococcu

293 RNA polymerase (RNAP) from thermophilic Thermus aquaticus is characterized by highe

294 tro at high temperature, making it the first thermophilic topoisomerase IB characterized so far.

295 (rRNA and tRNAs) in A. cellulolyticus showed thermophilic traits suggesting the importance of adaptat

296 us cellulolyticus CRISPR-Cas9 (AceCas9) is a thermophilic Type II-C enzyme that has potential genome

297 Synechococcus OS-B', a thermophilic unicellular cyanobacterium, recently isolat

298 Here, we purified an HAO from the thermophilic verrucomicrobial methanotroph Methylacidiph

299 the novel genomes, one belongs to a putative thermophilic virus infecting the bacterium Hydrogenobacu

300 ve C/D RNPs with recombinant proteins of the thermophilic yeast Chaetomium thermophilum.